Product image of Lenalidomid Axiromed (Lenalidomide) supplied by GNH India

Lenalidomid Axiromed

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomid Axiromed (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomid Axiromed, is an immunomodulatory drug presented as an oral formulation for oral use. It is employed in the treatment of certain blood cancers, particularly multiple myeloma and myelodysplastic syndromes, in adult patients.

GNH India supplies Lenalidomid Axiromed as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory documentation for importers. Its global logistics network ensures timely delivery across multiple regions.

Manufacturer / TM Owner

Medical Valley Invest Ab

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Indications & Clinical Uses

  • Lenalidomide is used as an antineoplastic agent targeting malignant plasma cells and dysplastic bone‑marrow clones.
  • Multiple myeloma: improves progression‑free survival and overall response when combined with dexamethasone or other agents.
  • Myelodysplastic syndromes with del(5q): reduces transfusion dependence and induces cytogenetic remission.

How It Works

  • Lenalidomide binds to the cereblon subunit of the CRL4‑E3 ubiquitin ligase complex, altering substrate specificity. This leads to ubiquitination and proteasomal degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), which suppresses malignant plasma‑cell proliferation, modulates cytokine production, enhances T‑cell and NK‑cell immunity, and inhibits angiogenesis within the bone‑marrow microenvironment.

Side Effects

Lenalidomide may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Fatigue
  • Neutropenia
  • Thrombocytopenia
  • Anemia
  • Constipation
  • Rash

Serious or Rare Side Effects

  • Venous thromboembolism (deep vein thrombosis, pulmonary embolism)
  • Severe neutropenia with infection risk
  • Secondary primary malignancies
  • Hypersensitivity reactions (including Stevens‑Johnson syndrome)
  • Cardiac arrhythmias
  • Hepatotoxicity

Precautions & Warnings

  • When prescribing lenalidomide, several safety considerations are required.
  • Pregnancy: contraindicated (Category X); avoid use in pregnant women.
  • Thrombosis risk: assess patient history and consider prophylactic anticoagulation.
  • Renal impairment: adjust dose based on renal function.
  • Hematologic monitoring: perform regular CBC to detect cytopenias.
  • Drug interactions: avoid concomitant use with strong CYP3A4 inhibitors.
  • Store at room temperature: keep below 25 °C, protect from moisture and light in original container.

Avoid Interactions

Lenalidomide can interact with other medicines, necessitating careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase lenalidomide exposure.
  • Live vaccines: risk of infection due to immunosuppression.
  • Thalidomide: additive teratogenic risk.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (warfarin, DOACs): increased bleeding risk.
  • CYP3A4 inducers (rifampin, phenytoin): may reduce efficacy.
  • Non‑live vaccines: monitor immune response.

Frequently Asked Questions

Lenalidomid Axiromed contains lenalidomide, which is indicated for the treatment of adult patients with multiple myeloma and for myelodysplastic syndromes that have a deletion of chromosome 5q. It is used as part of combination therapy to improve disease control and reduce transfusion needs.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This triggers degradation of transcription factors Ikaros and Aiolos, leading to reduced proliferation of malignant plasma cells, enhanced immune cell activity, and inhibition of new blood‑vessel formation in the bone‑marrow environment.

The specific dose and dosing schedule of Lenalidomid Axiromed are determined by the prescribing physician based on the patient’s condition, disease stage, renal function, and other clinical factors. The prescriber will set the appropriate regimen and adjust it as needed during therapy.

Lenalidomid Axiromed is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because it can cause severe fetal harm. It should not be used by nursing mothers, as it may be excreted in breast milk and pose a risk to the infant.

To request Lenalidomid Axiromed, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Lenalidomide is a second‑generation immunomodulatory agent, offering greater potency and a more favorable safety profile than thalidomide, while being less myelosuppressive than pomalidomide. It is often preferred when a balance between efficacy and tolerability is needed, especially in patients with del(5q) myelodysplastic syndromes.

Store Lenalidomid Axiromed at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children. Do not refrigerate or freeze the product.

Lenalidomid Axiromed is taken orally, usually with a glass of water. It may be taken with or without food, but the prescriber may give specific instructions to minimize gastrointestinal upset. Swallow the tablet whole; do not crush or split unless directed.

The most serious risks include severe neutropenia leading to infection, venous thromboembolism such as deep‑vein thrombosis or pulmonary embolism, and the potential development of secondary primary malignancies. Patients should be monitored closely for signs of infection, clotting events, and new cancers.

Lenalidomid Axiromed should not be used by pregnant women or women who may become pregnant, because of its teratogenicity. It is also contraindicated in patients with known hypersensitivity to lenalidomide or its excipients, and caution is required in those with severe renal impairment without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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